SHMARQL

epilepsy and/or ataxia with myoclonus as major feature

<http://www.wikidata.org/entity/Q55787253>

human disease
rdfs:label
"epilepsy and/or ataxia with myoclonus as major feature"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:01:42+00:00"^^xsd:dateTime
schema:version 2560161470
wikibase:identifiers 4
wikibase:sitelinks 0
wikibase:statements 8
p:P14914 wd:statement/Q55787253-256CC0AC-7F0F-451D-A2C9-DDFA6902311E
p:P1550 wd:statement/Q55787253-249C8DAA-A6B5-4C71-BD19-1E2B1C43F36D
p:P279 wd:statement/Q55787253-0F353CE7-312C-443C-9957-8B5D091F1B78
wd:statement/Q55787253-43E370C1-3382-4889-86CC-A4CA3B78FCF2
p:P2888 wd:statement/Q55787253-E0E04484-960F-4B74-9319-3F72AE3CFE53
p:P2892 wd:statement/Q55787253-880858F2-D731-4BD4-AC81-A11B78CDE8FC
p:P31 wd:statement/Q55787253-799F6713-67AA-44B8-99FD-210F16A5247E
p:P5270 wd:statement/Q55787253-208D1EA3-D767-4433-8DC3-36ECEFD9E85F
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0017653>
wdt:P14914 "D306756"
wdt:P1550 "306756"
wdt:P279 rare disease with myoclonus as a major feature
rare genetic disease with myoclonus as a major feature
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_306756>
wdt:P2892 "C5681050"
wdt:P31 type of disease
wdt:P5270 "MONDO_0017653"
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